Orphanet Journal of Rare Diseases

official impact factor 5.93
Search for
Advanced search
Orphanet Journal of Rare Diseases
Tools
Share this article
Open Access Highly Access

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome

Karine Morcel, Laure Camborieux, Programme de Recherches sur les Aplasies Müllériennes (PRAM) and Daniel Guerrier*

Orphanet Journal of Rare Diseases 2007, 2:13 doi:10.1186/1750-1172-2-13

Accesses  

  • Last 30 days: 405 accesses
  • Last 365 days: 3532 accesses
  • All time: 14313 accesses

Cited by

BioMed Central: 2 citations

Review   Open Access Highly Accessed

VACTERL/VATER Association

Benjamin D Solomon Orphanet Journal of Rare Diseases 2011, 6:56 (16 August 2011)

Abstract | Full text | PDF | PubMed

Research   Open Access

Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports

Laura Bernardini, Stefania Gimelli, Cristina Gervasini, Massimo Carella, Anwar Baban, Giada Frontino, Giancarlo Barbano, Maria Divizia, Luigi Fedele, Antonio Novelli, Frédérique Béna, Faustina Lalatta, Monica Miozzo, Bruno Dallapiccola Orphanet Journal of Rare Diseases 2009, 4:25 (4 November 2009)

Abstract | Full text | PDF | PubMed | Cited on BioMed Central

Google Scholar: View citations

ISI Web of Science: View citations

PubMed Central: View citations